1) Anhui food and drug administrative system
安徽省食品药品监督管理系统
1.
A stastistical analysis on the articles written by staff of Anhui food and drug administrative system from 2003 to 2007;
2003～2007年安徽省食品药品监督管理系统论文发表统计分析
3) drug administration
药品监督管理
1.
In order to exert the effect of medicine guild on Chinese drug administration,medicine guild has to be independent,and the relative law should be set up,that can ensure function of medicine guild,perfect itself and aware of the competition,etc.
在协助国家药品监督管理工作中发挥积极作用。
2.
Based on relevant theories in the Administrative Law, th e authors demonstrated and analyzed current drug administration practice, and su ggested to regulate discretional acts in drug administration by following up sui table principles and taking some measures.
文章在对行政法中相关理论进行阐述的基础上 ,结合药品监督管理实践进行论证分析 ,认为把握适当原则、采取一定措施 ,对药品监督管理中的裁量行为进行规范 ,有益于裁量行政行为的合理实施。
3.
To carry out and perfect the responsibility system in dr ug law administration is an important measure for drug administration units, esp ecially those under provincial level to strengthen responsibility, make legal ma nagement.
药品监督管理行政执法责任制的全面推行和完善 ,是药品监管机关、特别是地方省以下各级机关 ,强化药品监管行政责任 ,严格依法行政的重要保障措施。
4) FDA
[英][,ef di: 'eɪ] [美]['ɛf 'di 'e]
美国食品药品监督管理局
1.
According to USA FDA,and EU EC,EMEA,and FVO related regulations,this paper introduced the basic registration requirements of Chinese Traditional Medicine to apply marketing authorization in USA and EU.
参阅美国食品药品监督管理局(FDA,Food and Drug Administration);欧盟委员会(EC,European Commis-sion);欧盟药品审评局(EMEA,The European Agency for the Evaluation of Medicinal Products)及欧盟食品兽医办公室(FVO,Food and Veterinary Office)有关法律法规文件,就中药在欧美国家申请上市注册的基本要求做简要介绍。
2.
Briefly introduce the problems that FDA of America is facing related to drug risk man-agement as well as solutions to the system in order to explore effective approaches of drug risk management.
通过介绍美国食品药品监督管理局面临的药品风险管理问题及改进建议,以便探索对我国有借鉴意义的药品风险管理模式。
3.
This text followed the working progress after Drug Safety Oversight Board (DSOB) of FDA established.
通过跟踪美国食品药品监督管理局新成立的“药品安全监督委员会”的工作进展,了解其近期开展的工作内容和程序,以期对我国的药品风险管理体系建设和完善有所启示。
6) Drug Administration System
药品监督管理体制
补充资料：省可
1.谓批阅定夺。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条